Variant report
Variant | rs73366394 |
---|---|
Chromosome Location | chr21:17711708-17711709 |
allele | G/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
No data |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs13433500 | 1.00[EUR][1000 genomes] |
rs1492951 | 1.00[EUR][1000 genomes] |
rs1492958 | 1.00[EUR][1000 genomes] |
rs1689046 | 1.00[EUR][1000 genomes] |
rs16994578 | 1.00[EUR][1000 genomes] |
rs16994668 | 1.00[EUR][1000 genomes] |
rs16994829 | 1.00[EUR][1000 genomes] |
rs16994966 | 1.00[EUR][1000 genomes] |
rs1786832 | 1.00[EUR][1000 genomes] |
rs1786833 | 1.00[EUR][1000 genomes] |
rs239069 | 1.00[EUR][1000 genomes] |
rs239077 | 1.00[EUR][1000 genomes] |
rs2823640 | 1.00[EUR][1000 genomes] |
rs2823645 | 1.00[EUR][1000 genomes] |
rs2823649 | 1.00[EUR][1000 genomes] |
rs2823655 | 1.00[EUR][1000 genomes] |
rs2823656 | 1.00[EUR][1000 genomes] |
rs2823663 | 1.00[EUR][1000 genomes] |
rs2823664 | 1.00[EUR][1000 genomes] |
rs2823665 | 1.00[EUR][1000 genomes] |
rs2823666 | 1.00[EUR][1000 genomes] |
rs2823667 | 1.00[EUR][1000 genomes] |
rs2823668 | 1.00[EUR][1000 genomes] |
rs2823670 | 1.00[EUR][1000 genomes] |
rs2823673 | 1.00[EUR][1000 genomes] |
rs2823680 | 1.00[EUR][1000 genomes] |
rs2823681 | 1.00[EUR][1000 genomes] |
rs2823686 | 1.00[EUR][1000 genomes] |
rs2823689 | 1.00[EUR][1000 genomes] |
rs2823690 | 1.00[EUR][1000 genomes] |
rs2823691 | 1.00[EUR][1000 genomes] |
rs2823693 | 1.00[EUR][1000 genomes] |
rs2823694 | 1.00[EUR][1000 genomes] |
rs2823698 | 1.00[EUR][1000 genomes] |
rs2823701 | 1.00[EUR][1000 genomes] |
rs2823706 | 1.00[EUR][1000 genomes] |
rs2823714 | 1.00[EUR][1000 genomes] |
rs2823719 | 1.00[EUR][1000 genomes] |
rs2823723 | 1.00[EUR][1000 genomes] |
rs2823724 | 1.00[EUR][1000 genomes] |
rs2823726 | 1.00[EUR][1000 genomes] |
rs2823727 | 1.00[EUR][1000 genomes] |
rs2823728 | 1.00[EUR][1000 genomes] |
rs28379017 | 1.00[EUR][1000 genomes] |
rs28401314 | 1.00[EUR][1000 genomes] |
rs55909634 | 1.00[EUR][1000 genomes] |
rs55941929 | 1.00[EUR][1000 genomes] |
rs57097865 | 1.00[EUR][1000 genomes] |
rs58869062 | 1.00[EUR][1000 genomes] |
rs59964313 | 1.00[EUR][1000 genomes] |
rs60949090 | 1.00[EUR][1000 genomes] |
rs60963357 | 1.00[EUR][1000 genomes] |
rs61333624 | 1.00[EUR][1000 genomes] |
rs61414956 | 1.00[EUR][1000 genomes] |
rs6517694 | 1.00[EUR][1000 genomes] |
rs7275189 | 1.00[EUR][1000 genomes] |
rs7278407 | 1.00[EUR][1000 genomes] |
rs73357138 | 1.00[EUR][1000 genomes] |
rs73364854 | 1.00[EUR][1000 genomes] |
rs73364899 | 1.00[EUR][1000 genomes] |
rs73364901 | 1.00[EUR][1000 genomes] |
rs73368220 | 1.00[EUR][1000 genomes] |
rs73368227 | 1.00[EUR][1000 genomes] |
rs8126809 | 1.00[EUR][1000 genomes] |
rs8128157 | 1.00[EUR][1000 genomes] |
rs8134616 | 1.00[EUR][1000 genomes] |
rs9975784 | 1.00[EUR][1000 genomes] |
rs9977577 | 1.00[EUR][1000 genomes] |
rs9977984 | 1.00[EUR][1000 genomes] |
rs9981526 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv834051 | chr21:17564843-17721764 | Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
2 | nsv1064857 | chr21:17628760-18533131 | Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 345 gene(s) | inside rSNPs | diseases |
3 | nsv544382 | chr21:17628760-18533131 | Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 345 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr21:17701800-17724400 | Weak transcription | Psoas Muscle | Psoas |
2 | chr21:17703200-17712000 | Weak transcription | Hela-S3 | cervix |
3 | chr21:17703400-17722200 | Weak transcription | Ovary | ovary |
4 | chr21:17708200-17713000 | Weak transcription | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
5 | chr21:17709400-17723800 | Weak transcription | H9 Derived Neuron Cultured Cells | ES cell derived |